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Demyelinating and thrombotic diseases of the central nervous system: common pathogenic and triggering factors.中枢神经系统脱髓鞘疾病和血栓形成性疾病:常见的致病因素和触发因素。
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本文引用的文献

1
Studies on the Coagulation Defect in a Case of Thrombocytopenic Purpura Complicated by Thrombosis.血小板减少性紫癜合并血栓形成病例的凝血缺陷研究。
Am J Pathol. 1946 Nov;22(6):1181-203.
2
Circulating anticoagulant as a cause of hemorrhagic diathesis in man.循环抗凝物质作为人类出血素质的一个原因。
Bull Johns Hopkins Hosp. 1948 Oct;83(4):288-96.
3
Clinical utility of laboratory tests used to identify antiphospholipid antibodies and to diagnose the antiphospholipid syndrome.用于鉴定抗磷脂抗体和诊断抗磷脂综合征的实验室检测的临床效用。
Semin Thromb Hemost. 2008 Jun;34(4):329-34. doi: 10.1055/s-0028-1085474. Epub 2008 Sep 23.
4
A quarter of a century in anticardiolipin antibody testing and attempted standardization has led us to here, which is?二十五年的抗心磷脂抗体检测及标准化尝试把我们带到了这里,而这里是哪里呢?
Semin Thromb Hemost. 2008 Jun;34(4):313-28. doi: 10.1055/s-0028-1085473. Epub 2008 Sep 23.
5
Neurologic symptoms as a feature of the antiphospholipid syndrome.神经系统症状作为抗磷脂综合征的一个特征。
Semin Thromb Hemost. 2008 Apr;34(3):286-9. doi: 10.1055/s-0028-1082273.
6
Antiphospholipid antibodies and the antiphospholipid syndrome: pathogenic mechanisms.抗磷脂抗体与抗磷脂综合征:致病机制
Semin Thromb Hemost. 2008 Apr;34(3):236-50. doi: 10.1055/s-0028-1082267.
7
Thrombophilic dimension of recurrent fetal loss in Indian patients.印度患者复发性胎儿丢失的血栓形成倾向方面
Blood Coagul Fibrinolysis. 2008 Sep;19(6):581-4. doi: 10.1097/MBC.0b013e328304dffc.
8
Theodore E. Woodward Award: antiphospholipid syndrome revisited: a disorder initiated by inflammation.西奥多·E·伍德沃德奖:再探抗磷脂综合征:一种由炎症引发的疾病
Trans Am Clin Climatol Assoc. 2007;118:99-114.
9
Microparticle-mediated thrombin generation assay: increased activity in patients with recurrent thrombosis.微粒介导的凝血酶生成测定:复发性血栓形成患者的活性增加。
J Thromb Haemost. 2008 Jun;6(6):913-9. doi: 10.1111/j.1538-7836.2008.02963.x. Epub 2008 Mar 21.
10
Proteomic analysis of active multiple sclerosis lesions reveals therapeutic targets.对活动性多发性硬化症病灶的蛋白质组学分析揭示了治疗靶点。
Nature. 2008 Feb 28;451(7182):1076-81. doi: 10.1038/nature06559. Epub 2008 Feb 17.

抗磷脂抗体:处于转变中的范例。

Antiphospholipid antibodies: paradigm in transition.

作者信息

Horstman Lawrence L, Jy Wenche, Bidot Carlos J, Ahn Yeon S, Kelley Roger E, Zivadinov Robert, Maghzi Amir H, Etemadifar Masoud, Mousavi Seyed Ali, Minagar Alireza

机构信息

Department of Neurology, Louisiana State University Health Sciences Center, Shreveport, LA 71130, USA.

出版信息

J Neuroinflammation. 2009 Jan 20;6:3. doi: 10.1186/1742-2094-6-3.

DOI:10.1186/1742-2094-6-3
PMID:19154576
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2640381/
Abstract

OBJECTIVES

This is a critical review of anti-phospholipid antibodies (aPL). Most prior reviews focus on the aPL syndrome (APS), a thrombotic condition often marked by neurological disturbance. We bring to attention recent evidence that aPL may be equally relevant to non-thrombotic autoimmune conditions, notably, multiple sclerosis and ITP.

ORGANIZATION

After a brief history, the recent proliferation of aPL target antigens is reviewed. The implication is that many more exist. Theories of aPL in thrombosis are then reviewed, concluding that all have merit but that aPL may have more diverse pathological consequences than now recognized. Next, conflicting results are explained by methodological differences. The lupus anticoagulant (LA) is then discussed. LA is the best predictor of thrombosis, but why this is true is not settled. Finally, aPL in non-thrombotic disorders is reviewed.

CONCLUSION

The current paradigm of aPL holds that they are important in thrombosis, but they may have much wider clinical significance, possibly of special interest in neurology.

摘要

目的

这是一篇关于抗磷脂抗体(aPL)的批判性综述。大多数先前的综述聚焦于抗磷脂综合征(APS),这是一种常伴有神经功能障碍的血栓形成性疾病。我们提请注意最近的证据,即aPL可能与非血栓形成性自身免疫性疾病同样相关,特别是多发性硬化症和免疫性血小板减少症(ITP)。

组织架构

在简要介绍历史之后,回顾了最近aPL靶抗原的大量增加。这意味着可能还存在更多的靶抗原。接着回顾了aPL在血栓形成中的理论,得出的结论是所有理论都有其价值,但aPL可能具有比目前所认识到的更多样化的病理后果。接下来,通过方法学差异解释了相互矛盾的结果。然后讨论了狼疮抗凝物(LA)。LA是血栓形成的最佳预测指标,但为何如此尚未定论。最后,综述了aPL在非血栓形成性疾病中的情况。

结论

目前关于aPL的范式认为它们在血栓形成中很重要,但它们可能具有更广泛的临床意义,可能在神经病学领域具有特殊意义。